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4. The DNA deletion in an Indian delta beta-thalassaemia begins one kilobase from the A gamma globin gene and ends in an L1 repetitive sequence. Mishima N, Landman H, Huisman TH, Gilman JG. Br J Haematol; 1989 Nov; 73(3):375-9. PubMed ID: 2605124 [Abstract] [Full Text] [Related]
5. Gamma delta beta-thalassemia due to a de novo mutation deleting the 5' beta-globin gene activation-region hypersensitive sites. Driscoll MC, Dobkin CS, Alter BP. Proc Natl Acad Sci U S A; 1989 Oct; 86(19):7470-4. PubMed ID: 2798417 [Abstract] [Full Text] [Related]
7. The 3' breakpoint of the yunnanese (Agammadeltabeta)0-thalassemia deletion lies in an L1 family sequence: implications for the mechanism of deletion and the reactivation of the Ggamma-globin gene. Zhang XQ, Zhang JW. Hum Genet; 1998 Jul; 103(1):90-5. PubMed ID: 9737783 [Abstract] [Full Text] [Related]
12. Australian beta zero-thalassaemia: a high haemoglobin A2 beta zero-thalassaemia due to a 12 kb deletion commencing 5' to the beta-globin gene. Motum PI, Lindeman R, Hamilton TJ, Trent RJ. Br J Haematol; 1992 Sep; 82(1):107-13. PubMed ID: 1419783 [Abstract] [Full Text] [Related]
15. Rapid detection of Spanish (delta beta)zero-thalassemia deletion by polymerase chain reaction. Vives-Corrons JL, Pujades MA, Miguel-García A, Miguel-Sosa A, Cambiazzo S. Blood; 1992 Sep 15; 80(6):1582-5. PubMed ID: 1520881 [Abstract] [Full Text] [Related]
16. Partial deletion of beta-globin gene DNA in certain patients with beta 0-thalassemia. Orkin SH, Old JM, Weatherall DJ, Nathan DG. Proc Natl Acad Sci U S A; 1979 May 15; 76(5):2400-4. PubMed ID: 287080 [Abstract] [Full Text] [Related]
17. Heterogeneity of DNA deletion in gamma delta beta-thalassemia. Orkin SH, Goff SC, Nathan DG. J Clin Invest; 1981 Mar 15; 67(3):878-84. PubMed ID: 6162860 [Abstract] [Full Text] [Related]
18. Polymorphism of DNA sequence in the beta-globin gene region. Application to prenatal diagnosis of beta 0 thalassemia in Sardinia. Kan YW, Lee KY, Furbetta M, Angius A, Cao A. N Engl J Med; 1980 Jan 24; 302(4):185-8. PubMed ID: 6927915 [Abstract] [Full Text] [Related]
19. A spontaneous deletion of beta 33/34 Val in exon 2 of the beta globin gene (Hb Korea) produces the phenotype of dominant beta thalassaemia. Park SS, Barnetson R, Kim SW, Weatherall DJ, Thein SL. Br J Haematol; 1991 Aug 24; 78(4):581-2. PubMed ID: 1911355 [No Abstract] [Full Text] [Related]
20. The 12.6 kilobase DNA deletion in Dutch beta zero-thalassaemia. Gilman JG. Br J Haematol; 1987 Nov 24; 67(3):369-72. PubMed ID: 3689700 [Abstract] [Full Text] [Related] Page: [Next] [New Search]